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2-amino-5-methyl-6-phenylpyrimidin-4(1H)-one is a heterocyclic organic compound characterized by a pyrimidine ring structure. It features an amino group at the 2nd position, a methyl group at the 5th position, and a phenyl group at the 6th position. 2-amino-5-methyl-6-phenylpyrimidin-4(1H)-one is a derivative of pyrimidin-4(1H)-one, which is a parent compound of various biologically active molecules. The presence of the amino and methyl groups contributes to its potential reactivity and its ability to form hydrogen bonds, which can be significant in medicinal chemistry and drug design. The phenyl group provides additional structural complexity and can influence the compound's lipophilicity and interaction with biological targets. This chemical's structure and properties make it a candidate for further exploration in the development of new pharmaceuticals or as a building block in organic synthesis.

4987-28-4

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4987-28-4 Usage

Structure

Heterocyclic compound with a pyrimidine ring

Functional Groups

Amino group (-NH2) at the 2-position
Methyl group (-CH3) at the 5-position
Phenyl group (-C6H5) at the 6-position
Carbonyl group (C=O) at the 4-position

Synonym

AMP

Usage

Synthetic intermediate in pharmaceuticals, agrochemicals, and dyes production

Biological Activities

Antiviral
Anti-tumor
Cytotoxic effects

Importance in Medicinal Chemistry

Valuable molecule for medicinal chemistry research

Reactivity

Unique structure and reactivity

Applications

Building block for the synthesis of more complex compounds
Diverse applications in pharmaceuticals, agrochemicals, and dye industries

Check Digit Verification of cas no

The CAS Registry Mumber 4987-28-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4987-28:
(6*4)+(5*9)+(4*8)+(3*7)+(2*2)+(1*8)=134
134 % 10 = 4
So 4987-28-4 is a valid CAS Registry Number.

4987-28-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-5-methyl-6-phenylpyrimidin-4(3H)-one

1.2 Other means of identification

Product number -
Other names 2-amino-5-methyl-6-phenyl-3H-pyrimidin-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4987-28-4 SDS

4987-28-4Relevant academic research and scientific papers

Synthesis of 6-arylisocytosines and their potential for hydrogen bonding interactions

Patel, Alpa,Lewis, William,Searle, Mark S.,Stevens, Malcolm F.G.,Moody, Christopher J.

supporting information, p. 7339 - 7343 (2015/08/24)

Abstract The synthesis of a number of 6-arylisocytosines, including linked bis-isocytosines, from the reaction of guanidine with β-ketoesters is described. The compounds were investigated for their ability to form hydrogen-bonded structural networks, and for their potential interactions with the telomeric quadruplex forming sequence AGGG(TTAGGG)3.

Application of primary allylamines from morita-baylis-hillman adducts: Cyanogen azide mediated synthesis of substituted 5-aminotetrazoles and their attempted transformation into tetrazolo[1,5-a]pyrimidinones

Nag, Somnath,Bhowmik, Subhendu,Gauniyal, Harsh M.,Batra, Sanjay

supporting information; experimental part, p. 4705 - 4712 (2010/10/19)

A general protocol for the synthesis of substituted 5-aminotetrazoles by treating cyanogen azide with primary allylamines afforded either by S N2 or SN2′ reactions of Morita- Baylis-Hillman acetates of acrylate has been developed. Th

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